A Novel Model of Lethal Hendra Virus Infection in African Green Monkeys and the Effectiveness of Ribavirin Treatment

Author:

Rockx Barry1,Bossart Katharine N.23,Feldmann Friederike1,Geisbert Joan B.245,Hickey Andrew C.6,Brining Douglas7,Callison Julie1,Safronetz David1,Marzi Andrea1,Kercher Lisa7,Long Dan7,Broder Christopher C.6,Feldmann Heinz1,Geisbert Thomas W.2345

Affiliation:

1. Laboratory of Virology

2. National Emerging Infectious Diseases Laboratories Institute

3. Department of Microbiology, Boston University School of Medicine, 620 Albany Street, Boston, Massachusetts

4. Galveston National Laboratory

5. Department of Microbiology and Immunology, University of Texas Medical Branch, 301 University Blvd., Galveston, Texas

6. Department of Microbiology and Immunology, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, Maryland

7. Rocky Mountain Veterinary Branch, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 903 S. 4th Street, Hamilton, Montana

Abstract

ABSTRACT The henipaviruses, Hendra virus (HeV) and Nipah virus (NiV), are emerging zoonotic paramyxoviruses that can cause severe and often lethal neurologic and/or respiratory disease in a wide variety of mammalian hosts, including humans. There are presently no licensed vaccines or treatment options approved for human or veterinarian use. Guinea pigs, hamsters, cats, and ferrets, have been evaluated as animal models of human HeV infection, but studies in nonhuman primates (NHP) have not been reported, and the development and approval of any vaccine or antiviral for human use will likely require efficacy studies in an NHP model. Here, we examined the pathogenesis of HeV in the African green monkey (AGM) following intratracheal inoculation. Exposure of AGMs to HeV produced a uniformly lethal infection, and the observed clinical signs and pathology were highly consistent with HeV-mediated disease seen in humans. Ribavirin has been used to treat patients infected with either HeV or NiV; however, its utility in improving outcome remains, at best, uncertain. We examined the antiviral effect of ribavirin in a cohort of nine AGMs before or after exposure to HeV. Ribavirin treatment delayed disease onset by 1 to 2 days, with no significant benefit for disease progression and outcome. Together our findings introduce a new disease model of acute HeV infection suitable for testing antiviral strategies and also demonstrate that, while ribavirin may have some antiviral activity against the henipaviruses, its use as an effective standalone therapy for HeV infection is questionable.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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